Evidence map›Paper›PMID 27196776›Full record

ArticleMolecular cancer therapeutics2016

Secretory TRAIL-Armed Natural Killer Cell-Based Therapy: In Vitro and In Vivo Colorectal Peritoneal Carcinomatosis Xenograft.

Xinxin Song, Se-Hoon Hong, William T Kwon, Lisa M Bailey, Per Basse, David L Bartlett, Yong Tae Kwon, Yong J Lee

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 4 countries.

Xinxin SongDepartment of Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Se-Hoon HongDepartment of Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
William T KwonDepartment of Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Lisa M BaileyDepartment of Immunology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Per BasseDepartment of Immunology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
David L BartlettDepartment of Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Yong Tae KwonProtein Metabolism Medical Research Center and Department of Biomedical Science, College of Medicine, Seoul National University, Seoul, Korea.
Yong J LeeDepartment of Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania. Department of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania. leeyj@upmc.edu.
University of Pittsburgh · USSeoul National University · KR

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Multimodality approach to hepatic colorectal metastasesR01CA140554 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BARTLETT, DAVID L, LEE, YONG J · 2010 to 2014
$1.6M
NCI NIH HHS P30 CA047904NCI NIH HHS R01 CA140554
6 · The paper itself

Abstract

Since its discovery in 1995, TNF-related apoptosis-inducing ligand (TRAIL) has sparked growing interest among oncologists due to its remarkable ability to induce apoptosis in malignant human cells, but not in most normal cells. However, one major drawback is its fast clearance rate in vivo Thus, the development of an alternative means of delivery may increase the effectiveness of TRAIL-based therapy. In this study, we developed a secretory TRAIL-armed natural killer (NK) cell-based therapy and assessed its cytotoxic effects on colorectal cancer cells and its tumoricidal efficacy on colorectal peritoneal carcinomatosis xenograft. We generated genetically modified NK cells by transduction with a lentiviral vector consisting of a secretion signal domain, a trimerization domain, and an extracellular domain of the TRAIL gene. These NK cells secreted a glycosylated form of TRAIL fusion protein that induced apoptotic death. Intraperitoneally, but not intravenously, injected NK cells effectively accumulated at tumor sites, infiltrated tumor tissue, induced apoptosis, and delayed tumor growth. These results shed light on the therapeutic potential of genetically engineered NK cells to treat peritoneal carcinomatosis. Mol Cancer Ther; 15(7); 1591-601. ©2016 AACR.

Indexed as

Immunotherapy, AdoptiveAnimalsApoptosisCell Line, TumorColorectal NeoplasmsCytotoxicity, ImmunologicDisease Models, AnimalGene OrderGenetic TherapyGenetic VectorsHumansKiller Cells, NaturalMaleMicePeritoneal NeoplasmsTNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing Ligand

Identifiers

PMID27196776
PMCPMC4936937
OpenAlexW2339885297

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.